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首页> 外文期刊>Development Growth and Differentiation >Spatio-temporal expression of Xenopus vasa homolog, XVLG1, in oocytes and embryos: the presence of XVLG1 RNA in somatic cells as well as germline cells
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Spatio-temporal expression of Xenopus vasa homolog, XVLG1, in oocytes and embryos: the presence of XVLG1 RNA in somatic cells as well as germline cells

机译:异常表达Xenopus Vasa同源物,XVLG1,卵母细胞和胚胎:体细胞和种系细胞中的XVLG1 RNA存在

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The expression of Xenopus vasa homolog or XVLG1 was examined in oocytes and embryos by whole-mount in situ hybridization and reverse transcription-polymerase chain reaction (RT-PCR). To confirm the results in embryos, both methods were also appliedto explants of germ plasm-bearing cells (GPBC) from 32-cell embryos and to those of partial embryos deprived of GPBC. By hybridization, XVLG1 ribonucleic acid (RNA) was shown to be present throughout the cytoplasm in oocytes at stages I-III, except for the mitochondrial cloud. It was barely recognizable in a portion of germline cells of embryos at specific stages, notwithstanding that XVLG1 protein was present in those cells almost throughout their life-span. A weak signal for the RNA was detectable insome of the presumptive primordial germ cells (pPGC, descendants of GPBC from the gastrula stage onward) from the late gastrula (stage 12) to the hatching tadpole stage (stage 33/34), and in some of the PGC at stages 49-50. The results for pPGC were confirmed by the hybridization of explants of GPBC at equivalent stages in control embryos. In contrast, XVLG1 RNA was detected in certain somatic cells of embryos until stage 46. These observations were supported in part by the results of RT-PCR for embryosand explants. The possible role of the product of XVLG1 was reconsidered given its presence in both germline and somatic cells.
机译:通过全部安装原位杂交和逆转录 - 聚合酶链反应(RT-PCR),在卵母细胞和胚胎中检测Xenopus Vasa同源物或XVLG1的表达。为了确认胚胎中的结果,还从32个细胞胚胎和剥夺GPBC剥夺的部分胚胎的含生物血管细胞(GPBC)的外植体。通过杂交,XVLG1核糖核酸(RNA)显示在阶段I-III的卵母细胞中的整个细胞质中存在,除了线粒体云。在特定阶段的一部分种系细胞中几乎无法识别,尽管XVLG1蛋白在整个寿命期间存在于这些细胞中。从晚期胃肠杆菌(第12阶段)到孵化蝌蚪阶段(第33/34阶段),可检测到推测原始生殖细胞(PPGC,从胃肠杆阶段的GPBC的后代的GPBC后代)的弱信号。 PGC在49-50阶段。通过对照胚胎的等同阶段的GPBC的外植体的杂交证实了PPGC的结果。相反,在胚胎的某些体细胞中检测到XVLG1 RNA直至第46阶段。这些观察结果部分地由RT-PCR用于胚胎和外植体的结果。 XVLG1产品的可能作用被重新考虑,鉴于其在种系和体细胞中存在。

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